Canonical Allele Identifier: CA357619629

Gene: PKD2

Linked Data

• MyVariant Identifiers: chr4:g.88967968C>G (hg19) ; chr4:g.88046816C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88046816C>G , CM000666.2:g.88046816C>G	GRCh38
NC_000004.11:g.88967968C>G , CM000666.1:g.88967968C>G	GRCh37
NC_000004.10:g.89186992C>G	NCBI36
NG_008604.1:g.44149C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.1494C>G MANE Select	ENSP00000237596.2:p.His498Gln
ENST00000237596.6:c.1494C>G	ENSP00000237596.2:p.His498Gln
ENST00000508588.5:c.-199+3359C>G	ENSP00000427131.1:n.-199+3359C>G
NM_000297.3:c.1494C>G	NP_000288.1:p.His498Gln
XM_011532028.1:c.1269C>G	XP_011530330.1:p.His423Gln
XM_011532029.1:c.774C>G	XP_011530331.1:p.His258Gln
XM_011532030.1:c.654C>G	XP_011530332.1:p.His218Gln
XR_244632.2:n.1589C>G
NR_156488.1:n.1581C>G
XM_011532028.2:c.1269C>G	XP_011530330.1:p.His423Gln
XM_011532030.2:c.654C>G	XP_011530332.1:p.His218Gln
NM_000297.4:c.1494C>G MANE Select	NP_000288.1:p.His498Gln
NR_156488.2:n.1593C>G